摘要
Rational electrode design unlocks the kinetic limitations of vanadium redox flow battery (VRFB). Herein, we present a one-step electrochemical oxidation strategy under mild acidic conditions to fabricate N-S co-doped graphite felt (GF@N-S) electrodes. This innovative approach achieves simultaneous in situ sulfonation and amination on carbon surface, constructing a hierarchical porous architecture with dual-active sites—a previously unreported configuration for VRFBs. Distinguished by its simplicity, scalability, and metal-free, our method circumvents cost limitations while suppressing hydrogen evolution side reactions. The GF@N-S electrode exhibits a remarkable triple synergy: (1) N-S co-doping significantly reduces charge-transfer resistance, (2) an optimized pore architecture enhances mass transport, and (3) a tailored electronic structure dramatically accelerates reaction kinetics. As a result, the electrode achieves remarkable energy efficiency of 85.8 % at 300 mA cm−2 and 75.0 % at 500 mA cm−2, outperforming even state-of-the-art metal/carbon-nanomaterial hybrids. Notably, it exhibits exceptional stability with negligible active-site degradation over 1000 cycles. This work establishes a transformative paradigm for non-metal electrode engineering, seamlessly integrating atomic-scale doping control with industrial-scale manufacturability, and propelling the development of sustainable, high-performance energy storage systems.
| 源语言 | 英语 |
|---|---|
| 期刊论文编号 | 119832 |
| 期刊 | Journal of Energy Storage |
| 卷 | 145 |
| DOI | |
| 出版状态 | 已出版 - 1 2月 2026 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 7 经济适用的清洁能源
学术指纹
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